Palladium-catalyzed desulfinative cross-couplings
The Suzuki–Miyaura reaction has undeniably revolutionized the art of synthesis, particularly in the pharmaceutical industry. However, the coupling of 2-pyridine boronic acids has long remained a challenge. In this context, our laboratory has recently reported the use of pyridyl and other heteroaryl...
Autors principals: | de Gombert, A, Willis, MC |
---|---|
Format: | Journal article |
Idioma: | English |
Publicat: |
Cell Press
2020
|
Ítems similars
-
Mechanistic studies of the palladium-catalyzed desulfinative cross-coupling of aryl bromides and (hetero)aryl sulfinate salts
per: de Gombert, A, et al.
Publicat: (2020) -
Palladium-catalysed desulfinative cross-coupling reactions: Leveraging mechanistic insights for reaction optimisation
per: De Gombert, A
Publicat: (2021) -
Reductant-free cross-electrophile synthesis of di(hetero)arylmethanes by palladium-catalyzed desulfinative C–C coupling
per: McKnight, J, et al.
Publicat: (2022) -
Palladium-catalyzed cross-couplings in the synthesis of agrochemicals
per: Yuxin Zhu, et al.
Publicat: (2022-12-01) -
Heterocyclic allylsulfones as latent heteroaryl nucleophiles in palladium-catalyzed cross-coupling reactions
per: Markovic, T, et al.
Publicat: (2018)